ORPHA:363300
Genetic intractable diarrhea of infancy
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic intractable diarrhea of infancy | |
| fr | Diarrhée intraitable de l'enfant d'origine génétique | |
| de | Intraktable Diarrhoe im Kindesalter, genetisch bedingte | |
| es | Diarrea intratable genético de la infancia | |
| it | Diarrea intrattabile genetica dell'infanzia | IDI |
| nl | Genetische hardnekkige diarree in de zuigelingentijd | |
| pt | Diarreia intratável genética da infância | |
| pl | Dziecięca biegunka oporna na leczenie uwarunkowana genetycznie | IDI |
| cs | Geneticky podmíněné nezvladatelné průjmy kojenců | IDI |
| uk | Генетично обумовлена невиліковна діарея немовлят | |
| zh | 婴儿遗传性难治性腹泻 | |
| tr | Süt çocuğu genetik inatçı ishali |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680980 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:165655Genetic intestinal disease
rare genetic diseases
Children (11):
- ORPHA:1670Chronic diarrhea with villous atrophy
- ORPHA:329242Congenital chronic diarrhea with protein-losing enteropathy
- ORPHA:714487Congenital diarrhea-chronic gastrointestinal inflammation-ocular dysgenesis syndrome
- ORPHA:103908Congenital sodium diarrhea
- ORPHA:92050Congenital tufting enteropathy
- ORPHA:137622Intractable diarrhea-choanal atresia-eye anomalies syndrome
- ORPHA:2290Microvillus inclusion disease
- ORPHA:714490PERCC1-related congenital intractable malabsorptive diarrhea
- ORPHA:522043Syndromic autoimmune enteropathy
- ORPHA:563708Syndromic congenital sodium diarrhea
- ORPHA:84064Trichohepatoenteric syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/363300
- This record as JSON: /data/d/363300.json